JPH04251427A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPH04251427A JPH04251427A JP41623090A JP41623090A JPH04251427A JP H04251427 A JPH04251427 A JP H04251427A JP 41623090 A JP41623090 A JP 41623090A JP 41623090 A JP41623090 A JP 41623090A JP H04251427 A JPH04251427 A JP H04251427A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- back coat
- coat layer
- powder
- particle size
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 47
- 239000000843 powder Substances 0.000 claims abstract description 26
- 239000002245 particle Substances 0.000 claims description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
- 239000006247 magnetic powder Substances 0.000 claims description 12
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 8
- 239000003973 paint Substances 0.000 description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 230000003746 surface roughness Effects 0.000 description 7
- 238000004804 winding Methods 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 235000019241 carbon black Nutrition 0.000 description 5
- 229940105289 carbon black Drugs 0.000 description 5
- 239000006229 carbon black Substances 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 229920005749 polyurethane resin Polymers 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229910017368 Fe3 O4 Inorganic materials 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000007790 scraping Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- 229910018404 Al2 O3 Inorganic materials 0.000 description 1
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- 229910002440 Co–Ni Inorganic materials 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- 229910017344 Fe2 O3 Inorganic materials 0.000 description 1
- 229910001030 Iron–nickel alloy Inorganic materials 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 241001422033 Thestylus Species 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ULBTUVJTXULMLP-UHFFFAOYSA-N butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCC ULBTUVJTXULMLP-UHFFFAOYSA-N 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- -1 isocyanate compounds Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- AJCDFVKYMIUXCR-UHFFFAOYSA-N oxobarium;oxo(oxoferriooxy)iron Chemical compound [Ba]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O AJCDFVKYMIUXCR-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
- 229910006496 α-Fe2 O3 Inorganic materials 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】この発明は、表面に磁性層を有す
る基体の裏面にバックコ−ト層を設けた磁気テ−プなど
の磁気記録媒体に関し、さらに詳しくは走行性に優れた
前記の磁気記録媒体に関する。[Field of Industrial Application] The present invention relates to a magnetic recording medium such as a magnetic tape having a back coat layer on the back side of a substrate having a magnetic layer on the surface thereof, and more particularly to a magnetic recording medium such as a magnetic tape having excellent running properties. Regarding recording media.
【0002】0002
【従来の技術】一般に、磁気テ−プ等の磁気記録媒体に
おいては、高速巻き取り時の巻き乱れやベ−スフィルム
の削れ等を効果的に防止して、走行性および耐久性を改
善するため、磁性層を有する基体の裏面に、カ−ボンブ
ラック、アルミナなどの非磁性粉末を含むバックコ−ト
層を設けることが行われている。(特開昭51−306
号、特開昭52−102004号)[Prior Art] In general, in magnetic recording media such as magnetic tapes, it is necessary to effectively prevent winding irregularities and scraping of the base film during high-speed winding to improve runnability and durability. Therefore, a back coat layer containing non-magnetic powder such as carbon black or alumina is provided on the back surface of a substrate having a magnetic layer. (Unexamined Japanese Patent Publication No. 51-306
No., Japanese Patent Publication No. 52-102004)
【0003】0003
【発明が解決しようとする課題】ところが、従来からバ
ックコ−ト層に使用されているカ−ボンブラック、アル
ミナなどの非磁性粉末は、粒径が非常に微細なため、表
面粗さが平滑になりすぎて、走行性の改善が充分でなか
ったり、あるいは形状が角張った形状であったり、長軸
と短軸との軸比が種々に異なるため、走行中に削れたり
して粉落ちが生じやすく、走行性がいまひとつ充分に改
善されないという難点がある。[Problems to be Solved by the Invention] However, the non-magnetic powders such as carbon black and alumina conventionally used for the back coat layer have very fine particle sizes, so the surface roughness is smooth. If the shape is too angular and the improvement in running performance is not sufficient, or if the shape is angular or the axis ratio between the long axis and the short axis is different, it may be scraped while running and cause powder to fall off. However, the problem is that the running performance is not sufficiently improved.
【0004】0004
【課題を解決するための手段】この発明はかかる現状に
鑑み種々検討を行った結果なされたもので、バックコ−
ト層中に、平均粒径が 0.1μmから 1.5μmの
範囲内にあって、粒度分布(D25/D75)が 1.
5以下の真球状の非磁性粉末を含有させることによって
、バックコ−ト層の表面に均一な微小突起を形成し、摩
擦係数を充分に低減して、走行性を充分に向上させたも
のである。[Means for Solving the Problems] This invention has been made as a result of various studies in view of the current situation.
In the layer, the average particle diameter is within the range of 0.1 μm to 1.5 μm, and the particle size distribution (D25/D75) is 1.
By containing true spherical non-magnetic powder with a diameter of 5 or less, uniform microprotrusions are formed on the surface of the back coat layer, the coefficient of friction is sufficiently reduced, and running properties are sufficiently improved. .
【0005】この発明において、バックコ−ト層中に含
有させる非磁性粉末は、平均粒径が0.1μmから 1
.5μmの範囲内にあって、粒度分布(D25/D75
)が 1.5以下の真球状のものであることが好ましく
、このような平均粒径で粒度分布が均一な真球状の非磁
性粉末をバックコ−ト層中に含有させると、表面粗さが
平滑になりすぎることもなく、バックコ−ト層表面に均
一な微小突起が形成され、これによって走行時における
空気の巻き込みが効果的に防止されて、巻き乱れが生じ
ることもなく、走行性が向上される。また、粒度分布が
均一な真球状の非磁性粉末を使用すると、走行中に削ら
れて粉落ちが生じるという問題もなく、さらに突起の高
さの制御が可能となるため、バックコ−ト層の凹凸によ
る磁性層への影響を充分に抑制することができる。In the present invention, the non-magnetic powder contained in the back coat layer has an average particle size of 0.1 μm to 1 μm.
.. Within the range of 5 μm, particle size distribution (D25/D75
) is preferably 1.5 or less, and if such a spherical nonmagnetic powder with an average particle size and uniform particle size distribution is included in the back coat layer, the surface roughness will be reduced. It does not become too smooth, and uniform microscopic protrusions are formed on the surface of the back coat layer, which effectively prevents air from being drawn in during running, and improves running performance without causing irregular winding. be done. In addition, by using true spherical non-magnetic powder with a uniform particle size distribution, there is no problem of powder falling off due to scraping during running, and the height of the protrusions can be controlled, so the backcoat layer can be The influence of unevenness on the magnetic layer can be sufficiently suppressed.
【0006】これに対し、平均粒径が 0.1μmより
小さいものを使用すると、バックコ−ト層の表面粗さが
平滑になり過ぎ、摩擦係数が増大して、走行性が低下す
る。
また、 1.5μmより大きいものを使用すると、たと
え真球状であっても非磁性粉末の脱落が多くなり、走行
系を汚染するため好ましくない。また、粒度分布(D2
5/D75)が 1.5より大きくなると、適度な走行
性の粒径であってもスクラッチ傷をつけることがあり、
走行性を充分に向上することができない。On the other hand, if particles with an average particle diameter of less than 0.1 μm are used, the surface roughness of the back coat layer becomes too smooth, the coefficient of friction increases, and running properties deteriorate. Furthermore, if a particle having a diameter larger than 1.5 μm is used, even if it is perfectly spherical, a large amount of non-magnetic powder will fall off, contaminating the running system, which is not preferable. In addition, particle size distribution (D2
5/D75) is larger than 1.5, scratches may occur even if the particle size has moderate runnability.
Running performance cannot be sufficiently improved.
【0007】このような非磁性粉末の具体例としては、
例えば、いずれも平均粒径が 0.1μmから 1.5
μmの範囲内にあって、粒度分布(D25/D75)が
1.5以下の真球状のシリカ粉末、ポリメチルメタア
クリレ−ト粉末、ベンゾグアナミン粉末などが好適なも
のとして使用され、なかでもシリカ粉末がより好ましく
使用される。また使用量はバックコ−ト層中に含有され
る全固形成分に対して3〜20重量%の範囲内にするの
が好ましく、少なすぎると走行時に巻き乱れが生じ、多
すぎると表面性が粗されてドロップアウトの原因になっ
たり、脱落したりする。Specific examples of such non-magnetic powders include:
For example, the average particle size is between 0.1μm and 1.5μm.
Spherical silica powder, polymethyl methacrylate powder, benzoguanamine powder, etc., which are within the range of μm and have a particle size distribution (D25/D75) of 1.5 or less, are preferably used. Powders are more preferably used. In addition, the amount used is preferably within the range of 3 to 20% by weight based on the total solid components contained in the back coat layer. Too little amount will cause uneven winding during running, and too much amount will cause surface roughness. This may cause them to drop out or drop out.
【0008】このようなバックコ−ト層の形成は、通常
、平均粒径が 0.1μmから 1.5μmの範囲内に
あって、粒度分布(D25/D75)が 1.5以下の
真球状の非磁性粉末を、充填剤、結合剤樹脂および有機
溶剤等とともに混合分散してバックコ−ト層用塗料を調
製し、これを予め磁性層を表面に形成したポリエステル
フィルムなどの基体の裏面に塗布し、乾燥して行われる
。このようにして形成されるバックコ−ト層の厚さは
0.1〜2.0 μmの範囲内にするのが好ましく、
0.3〜1.2 μmの範囲内にするのがより好ましい
。[0008] The formation of such a back coat layer is usually performed using true spherical particles with an average particle diameter in the range of 0.1 μm to 1.5 μm and a particle size distribution (D25/D75) of 1.5 or less. A back coat layer coating material is prepared by mixing and dispersing non-magnetic powder with a filler, a binder resin, an organic solvent, etc., and this is applied to the back surface of a substrate such as a polyester film on which a magnetic layer has been previously formed. , is done dry. The thickness of the back coat layer formed in this way is
It is preferably within the range of 0.1 to 2.0 μm,
More preferably, it is within the range of 0.3 to 1.2 μm.
【0009】ここで、使用される結合剤樹脂としては、
たとえば、繊維素系樹脂、塩化ビニル−酢酸ビニル系共
重合体、ポリウレタン系樹脂、フェノ−ル系樹脂、アミ
ノ系樹脂、イソシアネ−ト化合物、放射線感応性樹脂な
ど、通常、磁気記録媒体に使用されるものがいずれも単
独で、あるいは二種以上混合して使用される。[0009] Here, the binder resin used is as follows:
For example, cellulose resins, vinyl chloride-vinyl acetate copolymers, polyurethane resins, phenolic resins, amino resins, isocyanate compounds, radiation-sensitive resins, etc. are commonly used in magnetic recording media. Each of these can be used alone or in combination of two or more.
【0010】また、有機溶剤としては、メチルイソブチ
ルケトン、メチルエチルケトン、シクロヘキサノン、ト
ルエン、酢酸エチル、テトラヒドロフラン、ジメチルホ
ルムアミドなど従来一般に使用される有機溶剤がいずれ
も単独で、あるいは二種以上混合して使用される。[0010] As the organic solvent, conventionally commonly used organic solvents such as methyl isobutyl ketone, methyl ethyl ketone, cyclohexanone, toluene, ethyl acetate, tetrahydrofuran, and dimethyl formamide can be used alone or in combination of two or more. Ru.
【0011】なお、このバックコ−ト層中には潤滑剤、
分散剤、帯電防止剤など、通常使用されている添加剤を
任意に添加使用してもよい。[0011] Note that this back coat layer contains a lubricant,
Commonly used additives such as dispersants and antistatic agents may be optionally added.
【0012】基体の表面に形成される磁性層は、γ−F
e2 O3 粉末、Fe3 O4 粉末、Co含有γ−
Fe2 O3 粉末、Co含有Fe3 O4 粉末、C
rO2 粉末、バリウムフェライト粉末、Fe粉末、C
o粉末、Fe−Ni粉末などの磁性粉末を、従来一般に
使用される結合剤樹脂および有機溶剤等とともに混合分
散して磁性塗料を調製し、この磁性塗料を基体の表面に
塗布、乾燥するなどの方法で形成される他、Co、Ni
、Fe、Co−Ni合金、Co−Cr合金、Co−P、
Co−Ni−Pなどの強磁性材を、真空蒸着、イオンプ
レ−ティング、スパッタリング、メッキ等の手段によっ
て基体上に被着するなどの方法でも形成される。The magnetic layer formed on the surface of the substrate is made of γ-F
e2 O3 powder, Fe3 O4 powder, Co-containing γ-
Fe2 O3 powder, Co-containing Fe3 O4 powder, C
rO2 powder, barium ferrite powder, Fe powder, C
A magnetic paint is prepared by mixing and dispersing magnetic powder such as o powder, Fe-Ni powder, etc. with a binder resin and an organic solvent that are commonly used in the past, and this magnetic paint is applied to the surface of a substrate and dried. Co, Ni
, Fe, Co-Ni alloy, Co-Cr alloy, Co-P,
It can also be formed by depositing a ferromagnetic material such as Co--Ni--P on a substrate by means such as vacuum evaporation, ion plating, sputtering, or plating.
【0013】また、基体としては、ポリエステル、ポリ
アミド、ポリイミド、ポリアミドセルロ−ス系誘導体な
どの合成樹脂製フイルムおよび非磁性の金属フイルムな
どがいずれも好適に使用される。As the substrate, films made of synthetic resins such as polyester, polyamide, polyimide, polyamide cellulose derivatives, and non-magnetic metal films are preferably used.
【0014】[0014]
【実施例】次に、この発明の実施例について説明する。
実施例1
α−Fe磁性粉末(平均粒径 0.18μm
) 100
重量部 塩化ビニル−酢酸ビニル−ビニルアルコ
−ル共重合体(積水 11.2 〃
化学工業社製、エスレックA) ポリウレタン
樹脂(大日本インキ化学工業社製、T−5250)
8.8 〃 カ−ボンブラック(平均粒
径 0.024μm)
6.0 〃 α−Al2 O3
(平均粒径 0.25μm)
8.0 〃 ミリス
チン酸
3.0 〃 ステアリン酸−n−ブチル
3.0 〃 シクロヘキサノン
115.0 〃
トルエン
115.0 〃この組成物をサンドグラ
インダ−ミルにより充分に混練分散させた後、多官能性
ポリイソシアネ−ト化合物(日本ポリウレタン工業社製
、コロネ−トL)を5重量部加えて磁性塗料を調製した
。これを厚さ13μmのポリエステルフィルム上に乾燥
厚が 3.0μmになるように塗布、乾燥した後、カレ
ンダ−処理を行って磁性層を形成した。[Example] Next, an example of the present invention will be described. Example 1 α-Fe magnetic powder (average particle size 0.18 μm
) 100
Parts by weight Vinyl chloride-vinyl acetate-vinyl alcohol copolymer (Sekisui 11.2
Manufactured by Kagaku Kogyo Co., Ltd., S-LEC A) Polyurethane resin (manufactured by Dainippon Ink Chemical Co., Ltd., T-5250)
8.8 〃 Carbon black (average particle size 0.024 μm)
6.0 〃 α-Al2 O3
(Average particle size 0.25μm)
8.0 Myristic acid
3.0 n-butyl stearate
3.0 〃 Cyclohexanone
115.0 〃
toluene
115.0 After thoroughly kneading and dispersing this composition using a sand grinder mill, 5 parts by weight of a polyfunctional polyisocyanate compound (Coronate L, manufactured by Nippon Polyurethane Industries, Ltd.) was added to prepare a magnetic paint. did. This was applied onto a polyester film having a thickness of 13 μm to a dry thickness of 3.0 μm, dried, and then calendered to form a magnetic layer.
【0015】次いで、表面に磁性層を形成したポリエス
テルフィルムの裏面に、下記のバックコ−ト層用塗料を
塗布、乾燥して厚さ 0.8μmのバックコ−ト層を形
成し、所定の幅に裁断して磁気テ−プをつくった。
バックコ−ト層用塗料
カ−ボンブラック(キャボット社製;モ−グル
L、揮発分 33.0重量部
5.0%、吸油量60cc/100g ) カ−
ボンブラック( コロンビア社製;セバカルブMT−C
I 4.1 〃 、揮発分0、油
量41cc/100g ) α−Fe2 O3
1.4
〃 CaCO3
16.5 〃 ニトロセル
ロ−ス(旭化成社製、ニトロセルロ−スHIG 1)
18.0 〃 ポリウレタン樹脂(日本ポリ
ウレタン社製、N−2309) 20.
2 〃 多官能性ポリイソシアネ−ト化合物(
日本ポリウレタン工業 6.8 〃
社製;コロネ−トL)
シリカ粉末(平均粒径 1.0μm、粒度分布
1.2、真球状) 15 〃
シクロヘキサノン
300 〃 トルエン
300 〃Next, on the back side of the polyester film on which the magnetic layer was formed, the following paint for back coat layer was applied and dried to form a back coat layer with a thickness of 0.8 μm, and the paint was spread to a predetermined width. I cut it up and made magnetic tape. Paint for back coat layer Carbon black (manufactured by Cabot; Mogul L, volatile content 33.0 parts by weight)
5.0%, oil absorption 60cc/100g) Car
Bon Black (manufactured by Columbia; Sebacarb MT-C
I 4.1 〃, volatile content 0, oil amount 41cc/100g) α-Fe2 O3
1.4
〃 CaCO3
16.5 Nitrocellulose (manufactured by Asahi Kasei Corporation, Nitrocellulose HIG 1)
18.0 Polyurethane resin (manufactured by Nippon Polyurethane Co., Ltd., N-2309) 20.
2 〃 Polyfunctional polyisocyanate compound (
Japan Polyurethane Industry 6.8 〃
manufactured by Coronate L) Silica powder (average particle size 1.0 μm, particle size distribution 1.2, true spherical) 15
cyclohexanone
300 Toluene
300 〃
【0
016】実施例2
実施例1におけるバックコ−ト層用塗料の組成において
、シリカ粉末の使用量を15重量部から10重量部に変
更した以外は、実施例1と同様にしてバックコ−ト層を
形成し、磁気テ−プをつくった。0
Example 2 A back coat layer was prepared in the same manner as in Example 1, except that the amount of silica powder used in the composition of the paint for the back coat layer in Example 1 was changed from 15 parts by weight to 10 parts by weight. A magnetic tape was made.
【0017】実施例3
実施例1におけるバックコ−ト層用塗料の組成において
、シリカ粉末の使用量を15重量部から5重量部に変更
した以外は、実施例1と同様にしてバックコ−ト層を形
成し、磁気テ−プをつくった。Example 3 A back coat layer was prepared in the same manner as in Example 1 except that the amount of silica powder used was changed from 15 parts by weight to 5 parts by weight in the composition of the paint for the back coat layer in Example 1. was formed and a magnetic tape was made.
【0018】比較例1
実施例1におけるバックコ−ト層用塗料の組成において
、シリカ粉末を省いた以外は実施例1と同様にしてバッ
クコ−ト層を形成し、磁気テ−プをつくった。Comparative Example 1 A back coat layer was formed in the same manner as in Example 1 except that the silica powder was omitted from the composition of the paint for the back coat layer in Example 1, and a magnetic tape was produced.
【0019】比較例2
実施例1におけるバックコ−ト層用塗料の組成において
、シリカ粉末の使用量を15重量部から 2.5重量部
に変更した以外は、実施例1と同様にしてバックコ−ト
層を形成し、磁気テ−プをつくった。Comparative Example 2 A back coat was prepared in the same manner as in Example 1, except that the amount of silica powder used in the composition of the paint for the back coat layer in Example 1 was changed from 15 parts by weight to 2.5 parts by weight. A magnetic tape was prepared by forming a magnetic tape.
【0020】比較例3
実施例1におけるバックコ−ト層用塗料の組成において
、シリカ粉末の使用量を15重量部から 0.5重量部
に変更した以外は、実施例1と同様にしてバックコ−ト
層を形成し、磁気テ−プをつくった。Comparative Example 3 A back coat was prepared in the same manner as in Example 1, except that the amount of silica powder used in the composition of the paint for the back coat layer in Example 1 was changed from 15 parts by weight to 0.5 parts by weight. A magnetic tape was prepared by forming a magnetic tape.
【0021】各実施例および比較例で得られた磁気テ−
プについて、実機走行テストを走行速度 1.5m/s
ec および 2.7m/sec の各速度で行って磁
気テ−プの巻き乱れの有無を観察し、バックコ−ト層の
表面形状が磁性層に及ぼす影響を調べた。バックコ−ト
層の表面形状が磁性層に及ぼす影響は、バックコ−ト層
の形状による磁性層表面への凹凸の転移を測定して行っ
た。この測定は、WYKO社製;TOPO−3Dを使用
して、触針を接触させずに測定した表面粗さ、凹凸の凸
部の高さ、凹部の深さ、凸部から凹部までの距離、触針
を接触させて測定した表面粗さをそれぞれ測定した。[0021] The magnetic tape obtained in each example and comparative example
Regarding the drive, we conducted an actual machine running test at a running speed of 1.5 m/s.
The magnetic tape was tested at speeds of 2.7 m/sec and 2.7 m/sec to observe the presence or absence of winding disorder in the magnetic tape, and to examine the influence of the surface shape of the back coat layer on the magnetic layer. The effect of the surface shape of the back coat layer on the magnetic layer was determined by measuring the transition of irregularities on the surface of the magnetic layer due to the shape of the back coat layer. This measurement was performed using WYKO's TOPO-3D, which measured the surface roughness without contacting the stylus, the height of the convex part of the unevenness, the depth of the concave part, the distance from the convex part to the concave part, The surface roughness was measured by contacting with a stylus.
【0022】下記第1表はその結果である。Table 1 below shows the results.
【0023】[0023]
【発明の効果】上記第1表から明らかなように、比較例
1〜3で得られた磁気テ−プは巻き乱れが見られるのに
対し、実施例1〜3で得られた磁気テ−プは、巻き乱れ
がなく、また、実施例1〜3で得られた磁気テ−プは、
いずれも比較例1〜3で得られた磁気テ−プと同様に表
面粗さが同等で、バックコ−ト層の磁性層に及ぼす影響
が小さく、このことから平均粒径が 0.1μmから
1.5μmの範囲内にあって、粒度分布(D25/D7
5)が1.5以下の真球状非磁性粉末を含有したバック
コ−ト層を有するこの発明の磁気テ−プは、従来の磁気
テ−プに比べて、走行性が格段に向上されていることが
わかる。Effects of the Invention As is clear from Table 1 above, the magnetic tapes obtained in Comparative Examples 1 to 3 show winding disorder, whereas the magnetic tapes obtained in Examples 1 to 3 The magnetic tapes had no winding disorder, and the magnetic tapes obtained in Examples 1 to 3 had
All of them have the same surface roughness as the magnetic tapes obtained in Comparative Examples 1 to 3, and have little effect on the magnetic layer of the back coat layer. Therefore, the average particle size is 0.1 μm or less.
Within the range of 1.5 μm, particle size distribution (D25/D7
The magnetic tape of the present invention, which has a back coat layer containing true spherical non-magnetic powder with 5) of 1.5 or less, has significantly improved runnability compared to conventional magnetic tapes. I understand that.
Claims (2)
平均粒径が 0.1μmから 1.5μmの範囲内にあ
って、粒度分布(D25/D75)が 1.5以下の真
球状の非磁性粉末を含有するバックコ−ト層を設けたこ
とを特徴とする磁気記録媒体[Claim 1] On the back surface of a substrate having a magnetic layer on the surface,
It is characterized by providing a back coat layer containing true spherical non-magnetic powder with an average particle size within the range of 0.1 μm to 1.5 μm and a particle size distribution (D25/D75) of 1.5 or less. magnetic recording medium
る請求項1記載の磁気記録媒体2. The magnetic recording medium according to claim 1, wherein the spherical nonmagnetic powder is silica powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP41623090A JPH04251427A (en) | 1990-12-29 | 1990-12-29 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP41623090A JPH04251427A (en) | 1990-12-29 | 1990-12-29 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04251427A true JPH04251427A (en) | 1992-09-07 |
Family
ID=18524470
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP41623090A Withdrawn JPH04251427A (en) | 1990-12-29 | 1990-12-29 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04251427A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5510169A (en) * | 1994-10-14 | 1996-04-23 | Minnesota Mining And Manufacturing Company | Magnetic recording medium with backside coating containing polymeric particles |
US5607747A (en) * | 1994-04-15 | 1997-03-04 | Minnesota Mining And Manufacturing Company | Magnetic recording media having a backside coating which includes multicomponent, nonmagnetic particles |
-
1990
- 1990-12-29 JP JP41623090A patent/JPH04251427A/en not_active Withdrawn
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5607747A (en) * | 1994-04-15 | 1997-03-04 | Minnesota Mining And Manufacturing Company | Magnetic recording media having a backside coating which includes multicomponent, nonmagnetic particles |
US5510169A (en) * | 1994-10-14 | 1996-04-23 | Minnesota Mining And Manufacturing Company | Magnetic recording medium with backside coating containing polymeric particles |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
A300 | Application deemed to be withdrawn because no request for examination was validly filed |
Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 19980312 |